Allele Registry

Canonical Allele Identifier: PA2825096436

Gene: CFH HGNC NCBI

ClinVar Allele:

1151870

ClinVar RCV:

RCV001507513

ClinVar Variation:

1162888

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Arg257Cys	CA1305140 NM_000186.4:c.769C>T